US4906523A - Primer for surfaces containing inorganic oxide - Google Patents

Primer for surfaces containing inorganic oxide Download PDF

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Publication number
US4906523A
US4906523A US07/100,604 US10060487A US4906523A US 4906523 A US4906523 A US 4906523A US 10060487 A US10060487 A US 10060487A US 4906523 A US4906523 A US 4906523A
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United States
Prior art keywords
composite structure
solvent
intermediate layer
layer
bonded
Prior art date
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Expired - Lifetime
Application number
US07/100,604
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English (en)
Inventor
Zayn Bilkadi
Harald Guder
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3M Co
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Minnesota Mining and Manufacturing Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Priority to US07/100,604 priority Critical patent/US4906523A/en
Assigned to MINNESOTA MINING AND MANUFACTURING COMPANY reassignment MINNESOTA MINING AND MANUFACTURING COMPANY ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: BILKADI, ZAYN, GUDER, HARALD
Priority to CA 577228 priority patent/CA1329440C/en
Priority to JP23864288A priority patent/JP2756272B2/ja
Priority to ZA887156A priority patent/ZA887156B/xx
Priority to DE88308871T priority patent/DE3882108T2/de
Priority to EP19880308871 priority patent/EP0309276B1/de
Application granted granted Critical
Publication of US4906523A publication Critical patent/US4906523A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34—Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • E—FIXED CONSTRUCTIONS
    • E01—CONSTRUCTION OF ROADS, RAILWAYS, OR BRIDGES
    • E01F—ADDITIONAL WORK, SUCH AS EQUIPPING ROADS OR THE CONSTRUCTION OF PLATFORMS, HELICOPTER LANDING STAGES, SIGNS, SNOW FENCES, OR THE LIKE
    • E01F9/00—Arrangement of road signs or traffic signals; Arrangements for enforcing caution
    • E01F9/50—Road surface markings; Kerbs or road edgings, specially adapted for alerting road users
    • E01F9/506—Road surface markings; Kerbs or road edgings, specially adapted for alerting road users characterised by the road surface marking material, e.g. comprising additives for improving friction or reflectivity; Methods of forming, installing or applying markings in, on or to road surfaces
    • E01F9/512—Preformed road surface markings, e.g. of sheet material; Methods of applying preformed markings
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00—Coatings on glass
    • C03C2217/40—Coatings comprising at least one inhomogeneous layer
    • C03C2217/43—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
    • C03C2217/46—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
    • C03C2217/47—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase consisting of a specific material
    • C03C2217/475—Inorganic materials
    • C03C2217/478—Silica
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/254—Polymeric or resinous material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/256—Heavy metal or aluminum or compound thereof
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/256—Heavy metal or aluminum or compound thereof
    • Y10T428/257—Iron oxide or aluminum oxide
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/259—Silicic material
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31652—Of asbestos
    • Y10T428/31667—Next to addition polymer from unsaturated monomers, or aldehyde or ketone condensation product

Definitions

  • This invention relates to a composition that is a primer or adhesive for inorganic substrates.
  • it relates to a composite structure comprising, in sequence, a first member inorganic substrate, a second member primer layer, and a third member selected from a functional layer or a second inorganic substrate.
  • it relates to a method for making the composite structure.
  • Primer compositions that promote the adhesion of overcoatings onto substrates are known in the art. They are particularly useful in articles requiring the bonding of organic materials to inorganic substrates. The resulting adhesion of the overcoating, however, is frequently less than is necessary for the desired use.
  • Silica organosols have been added to organic polymer type protective coatings to strengthen and improve the adhesion of the coating to a substrate.
  • U.S. Pat. No. 2,692,867 discloses the use of silica organosols of silica particles having absorbed on their surface a long hydrocarbon chain substituted ammonium ion and
  • U.S. Pat. No. 2,801,185 discloses the use of silica particles having a coating of any substance reactive with the silica surface, preferably an alcohol. The use of such a composition is described only as the exposed coating itself and is not disclosed as a primer.
  • Antireflective coatings of inorganic oxides on optical articles are described in Assignees copending patent applications U.S. Ser. No. 035,272 filed Apr. 2, 1987 and U.S. Ser. No. 910,250 filed Sept. 19, 1986.
  • Coating compositions comprising a sol of a metal oxide and optionally a binder resin are disclosed. The use of these compositions as a primer is not disclosed.
  • the prior art does not teach a composition suitable for the rapid promotion of adhesion of a polymeric coating, e.g., paints, lacquers, tapes and the like onto inorganic surfaces, e.g., concrete, ceramics, porcelain, glass, bricks, stone, metal and the like or the adhesion of one inorganic substrate to another inorganic substrate.
  • a polymeric coating e.g., paints, lacquers, tapes and the like onto inorganic surfaces, e.g., concrete, ceramics, porcelain, glass, bricks, stone, metal and the like or the adhesion of one inorganic substrate to another inorganic substrate.
  • the present invention provides a composition that is a primer or adhesive (herein called "primer/adhesive") for the adherence of layers to metal oxide-containing substrates particularly silicon oxide-containing substrates and for the adherence of one metal oxide-containing substrate to another metal oxide-containing substrate.
  • the invention particularly provides a primer/adhesive for adherence of overcoating functional layers or metal oxide-containing substrates to metal oxide-containing substrates.
  • the primer/adhesive composition of the invention comprises a colloidal dispersion of:
  • thermoplastic elastomers that are
  • colloidal inorganic oxides particularly silicon dioxide, present as an organosol
  • the present invention also provides a composite structure comprising:
  • a first layer comprising a metal oxide-containing substrate, e.g., a highway, street, or path of hydraulic or asphaltic concrete, a concrete block wall; masonry materials including bricks, plaster, mortar, stucco, and stone; ceramics including first clay products, whitewares, enamels, refractories, porcelain, glass or tile,
  • a metal oxide-containing substrate e.g., a highway, street, or path of hydraulic or asphaltic concrete, a concrete block wall
  • masonry materials including bricks, plaster, mortar, stucco, and stone
  • ceramics including first clay products, whitewares, enamels, refractories, porcelain, glass or tile
  • a third layer usually having a specific functional objective, such as a protective coating, an abrasion resistant coating, a marking layer, a decorative layer, a lubricant layer and the like or another metal oxide-containing substrate.
  • metal oxide-containing substrate a substrate that comprises one or more metal oxides, i.e., silicon dioxide, calcium oxide, and aluminum oxide, that may also contain one or more of other elements present as an oxide including, for example, hydrogen, calcium, magnesium, barium, iron, nickel, beryllium, tin, titanium, copper and zirconium.
  • thermoplastic elastomer soluble in proton accepting solvents an elastomer, e.g., a polymer than can be stretched by tension within its limits of elastic deformation and on release of tension recovers at least about 90 percent of its original dimensions, that is soluble in a proton accepting solvent.
  • proton accepting solvent an organic compound having an electron configuration such that it will accept the hydrogen of a proton donating compound.
  • the proton accepting solvent of use in the invention preferably has a boiling point below 100° C., as for example, acetone, ethyl acetate, acetonitrile, and tetrahydrofuran.
  • the composition of the invention is excellently suitable for use in bonding traffic control stripes to highway and street surfaces, e.g., to its use with pavement-marking sheet materials.
  • the composition can be applied to the pavement even under conditions when the pavement is wet.
  • the elastomer-sol composition evidently bonds because much of the water present is carried off by the evaporating solvent.
  • High strength bonding of the composition apparently is obtained because of the formation of bonds between the inorganic metal oxide, especially silica, in the pavement material, and the inorganic metal oxide in the sol of the elastomer-sol composition where a network of metal oxide particles forms on disappearance of the hydroxyl group-containing solvent which had stabilized the dispersion of metal oxide sol in the composition.
  • the primer or adhesive composition of the invention provides for the adherence of overcoating functional layers to metal oxide containing substrates such as concrete including both hydraulic concrete and asphaltic concrete; masonry materials including cement block, bricks, plaster, mortar, stucco, stone; ceramics including fired clay products, whitewares, enamels, refractories, porcelain, glass, and tile; and metals, for example, steel, aluminum and copper.
  • substrates comprise, in common, one or more metal oxides such as silicon dioxide, aluminum oxide, zirconium oxide, calcium oxide, and iron oxide and can also contain one or more of the oxides and ions of any of the elements listed in the Periodic Table of Elements.
  • the metal oxide-containing substrate can furthermore contain materials that are not metal oxides such as organic polymers, e.g., asphaltic materials, fibers, flakes, graphite or metal wires, and rods that are added to the substrate for structural reinforcement or modification of characteristics of the substrate.
  • materials that are not metal oxides such as organic polymers, e.g., asphaltic materials, fibers, flakes, graphite or metal wires, and rods that are added to the substrate for structural reinforcement or modification of characteristics of the substrate.
  • thermoplastic elastomer of use in the primer/adhesive composition of the invention is one that is soluble at least to 10%, preferably at least to 20%, by weight in a proton accepting solvent (e.g., acetone) and does not swell in petroleum solvents nor absorb more than about 5 percent by weight of such petroleum solvents (e.g., hexane).
  • a proton accepting solvent e.g., acetone
  • polyester-polyurethanes examples include but are not limited to polyester-polyurethanes, polyether-polyurethanes, homopolymers and copolymers of acrylate esters such as poly(ethyl acrylate) and poly(ethyl acrylate-ethylene), nitrile rubbers such as poly(butadiene-acrylonitrile), chlorosulfonated polyolefins, and fluorocarbon elastomers.
  • the polyurethanes are preferred because of their toughness and oil resistance and the polyacrylates are preferred because of their stability in sunlight, resistance to oil, and enhanced hydrolytic stability.
  • polyester-polyurethanes examples include the EstaneTM resins of B.F. Goodrich Chemical Co.
  • Colloidal inorganic oxides utilized in the present invention are finely divided metal oxide particles having a particle size of less than about 400 Angstroms preferably less than 250 Angstroms, that are dispersed or suspended in water or an organic solvent. Generally such dispersions or suspensions are termed hydrosols when suspended in water and orgonosols when suspended in an organic solvent.
  • Preferred colloidal inorganic oxides are the oxides of silicon, aluminum, zirconium, chromium, and titanium of which the most preferred are the oxides of silicon.
  • dispersions of metal oxides include “Dispural” and “Pural” boehmite (Al 2 O 3 .H 2 0) available from Condea Petrochemie (GmbH: “Catapal” SB boehmite available from Vista Chemical Co.; "Nalco” ISJ-614 alumina sol, “Nalco” ISJ-613 alumina coated silica sol, “Nalco” 2326, “Nalco” 1034A, “Nalco” 1034A, “Nalco” 1129, and “Nalco” 8455-258 silica sols available from Nalco Chemical Co.; and “Ludox" LS silica sol available from E.I. duPont.
  • Proton accepting solvents useful in the compositions of the invention are those having a boiling point of 100° C. or lower, preferably of about 50 to 80° C.
  • solvents are ketones, nitriles, esters, and ethers such as acetone, acetonitrile, isobutyronitrile, diethyl ketone, methyl ethyl ketone, methyl n-propyl ketone, nitromethane, propionitrile, dimethoxyethane, ethyl acetate, ethyl propionate, methyl acetate, tetrahydrofuran and tetrahydroxyan.
  • Preferred proton accepting solvents are acetone, methyl ethyl ketone, and methyl t-butyl ether.
  • Hydroxy group-containing solvents useful in the composition of the invention are selected from water and alkanols that boil below about 125° C.
  • alkanols include methanol, ethanol, propanol, isopropanol, 2-ethoxyethanol, and 2-propoxyethanol.
  • the priming/adhesive composition of the invention is prepared by mixing or blending the organic sol with one or more thermoplastic elastomers in a mixture of one or more proton accepting solvents and one or more organic hydroxy group-containing solvents.
  • the materials may be mixed in any order.
  • the inorganic sol is present as a dispersion in a hydroxyl group-containing organic solvent, having been prepared or purchased in such a solvent, preferably at a concentration of from about 10 to about 35 percent by weight.
  • the dispersion is mixed into a solution of the thermoplastic elastomer in one or more organic proton accepting solvents that have a boiling point, preferably of 100° C. or less at atmospheric pressure and that is at a concentration of about 10 to 20 percent by weight of total solution.
  • Relative amounts of sol dispersions and elastomer solutions are chosen and additional solvents added or removed, as by volatilization, so that the resulting primer/adhesive composition preferably contains from about 0.5 to 10 parts of elastomer per part of colloidal inorganic oxide, from about 1 part to 10 parts of hydroxy group-containing solvent per part of colloidal inorganic oxide, and from about 5 to 30 parts of proton accepting solvent per part of elastomer. Water can also be present in the composition in an amount less than the amount which brings about the precipitation of elastomer from the composition.
  • the composition contains 2.5 to 5 parts of elastomer per part of colloidal inorganic oxide when the elastomer is an acrylic resin and about 1.0 to 2.5 parts of elastomer per part of colloidal inorganic oxide when the elastomer is a urethane rubber. These proportions with respect to 0.8 parts of colloidal inorganic oxide are preferred.
  • the primer/adhesive composition of the invention even when containing up to two parts of colloidal inorganic oxide remains clear for prolonged periods of time and does not form precipitates as do paints and varnishes containing larger inorganic oxide particles such as fumed silica.
  • the compositions furthermore dry to optically clear films when pigments, dyes, or other optical density-providing additives are absent.
  • Preparation of primer/adhesive composition Into a 150 ml. bottle was placed 20 g. of a 20% by weight solution of polyurethane elastomer in acetone (EstaneTM 5703 obtained from B.F. Goodrich) and 46.7 g. of acetone and the mixture was shaken well on a vibratory shaker. There was then added dropwise 13.3 g. of a 30% by weight silica sol (NalcoTM 1129 obtained from Nalco Chemical Co.) in 40/30 isopropanol/water while shaking the mixture. A clear solution having 10% by weight solids was obtained. The solution remained clear on prolonged standing. The solution contained 1 part of urethane elastomer, 1.3 parts of isopropanol per part per weight of colloidal silica, and 1 part of water and 19.6 parts of acetone per part of urethane elastomer.
  • Example 1 The procedure for Example 1 was repeated using only 33.4 g. instead of 46.7 g. acetone and 6.65 g. instead of 13.3 g. of silica sol. A clear solution having 10% by weight solids was obtained that remained clear on prolonged standing.
  • Per part by weight of colloidal silica there was 2 parts of urethane elastomer, 1.3 parts of isopropanol, and 1 part of water. There was 12.3 parts of acetone per part of urethane resin.
  • Pavement marking tape applied to concrete as described in Example 1 that had been primed with the primer required a force of about twice that to peel the tape from an unprimed block. Following removal of the tape, the underlying surface was clean and unmarked by elastomer or adhesive from the tape.
  • Example 2 The procedure of Example 1 was repeated using 40 g. of a 20% by weight solution of polyurethane elastomer, 53.3 g. of acetone, and 6.7 g. of 30% silica sol. A clear solution, 10% by weight in solids, was obtained that remained clear on prolonged standing.
  • the solution contained per part by weight of colloidal silica 4 parts of urethane rubber, 1.3 parts of isopropanol, and 1 part of water. These were 10.7 parts of acetone per part of urethane elastomer.
  • Example 2 Into 80 parts of acetone was dissolved 20 parts of a 41% acrylonitrile--59% butadiene copolymer (HycarTM 1022 available from B.F. Goodrich). Following the procedure of Example 1, to 20 g. of this solution was added 60 g. acetone and 13.3 g. of 30% by weight silica sol using vigorous shaking to break up lumps which initially formed. A translucent solution having 8.5% solids was obtained that contained per part of colloidal silica, one part of acrylic elastomer, 1.3 parts of isopropanol, and 1 part of water. There were 21 parts of acetone per part of acrylic rubber.
  • HycarTM 1022 available from B.F. Goodrich
  • the primer was applied to concrete as described in Example 1. It dried within 5 minutes to a clear transparent film which was extremely aggressive toward a pavement marking article comprising a bulk material of a polyethylene/acrylonitrile rubber with pigments and fillers and an adhesive of polybutadiene rubber (the article hereinafter referred to as the "standard" pavement marking).
  • Vamac® duPont's ethylene-methyl acrylate-copolymer
  • acetone 126.7 g. of acetone were added and the mixture shaken well on a vibratory mixer.
  • 13.3 g. of a 30% by weight silica colloid in 40/30 isopropanol/water solvent were added slowly to the shaken mixture and with continued mixing.
  • the resulting dispersion was clear, containing 10% solids. When coated on concrete in a cold room, it dried within 5 minutes and adhered very well to the block and aggressively formed a bond with standard pavement marking tape.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Materials Engineering (AREA)
  • Geochemistry & Mineralogy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Civil Engineering (AREA)
  • Architecture (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Paints Or Removers (AREA)
  • Laminated Bodies (AREA)
  • Aftertreatments Of Artificial And Natural Stones (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US07/100,604 1987-09-24 1987-09-24 Primer for surfaces containing inorganic oxide Expired - Lifetime US4906523A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
US07/100,604 US4906523A (en) 1987-09-24 1987-09-24 Primer for surfaces containing inorganic oxide
CA 577228 CA1329440C (en) 1987-09-24 1988-09-13 Primer for surfaces containing inorganic oxide
JP23864288A JP2756272B2 (ja) 1987-09-24 1988-09-22 無機酸化物含有表面用プライマー組成物
ZA887156A ZA887156B (en) 1987-09-24 1988-09-23 Primer for surfaces containing inorganic oxide
DE88308871T DE3882108T2 (de) 1987-09-24 1988-09-23 Zusammensetzung zum Grundieren von anorganisches Oxyd enthaltenden Oberflächen.
EP19880308871 EP0309276B1 (de) 1987-09-24 1988-09-23 Zusammensetzung zum Grundieren von anorganisches Oxyd enthaltenden Oberflächen

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/100,604 US4906523A (en) 1987-09-24 1987-09-24 Primer for surfaces containing inorganic oxide

Publications (1)

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US4906523A true US4906523A (en) 1990-03-06

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US07/100,604 Expired - Lifetime US4906523A (en) 1987-09-24 1987-09-24 Primer for surfaces containing inorganic oxide

Country Status (6)

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US (1) US4906523A (de)
EP (1) EP0309276B1 (de)
JP (1) JP2756272B2 (de)
CA (1) CA1329440C (de)
DE (1) DE3882108T2 (de)
ZA (1) ZA887156B (de)

Cited By (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5013621A (en) * 1990-04-23 1991-05-07 Minnesota Mining And Manufacturing Company One-part white reflective coating
WO1994000519A1 (en) * 1992-06-20 1994-01-06 Minnesota Mining And Manufacturing Company Priming composition for wet and dry road surfaces
US5304224A (en) * 1992-10-01 1994-04-19 Minnesota Mining And Manufacturing Company Coated abrasive article having a tear resistant backing
US5316812A (en) * 1991-12-20 1994-05-31 Minnesota Mining And Manufacturing Company Coated abrasive backing
US5355636A (en) * 1992-10-01 1994-10-18 Minnesota Mining And Manufacturing Company Tear resistant coated abrasive article
US5427842A (en) * 1992-10-01 1995-06-27 Minnesota Mining And Manufacturing Company Tear resistant multilayer films and articles incorporating such films
US5437912A (en) * 1991-10-11 1995-08-01 Minnesota Mining And Manufacturing Company Coated thin film for imaging
US5453320A (en) * 1990-10-31 1995-09-26 Minnesota Mining And Manufacturing Company Pavement marking material
US5551961A (en) * 1992-09-15 1996-09-03 Minnesota Mining And Manufacturing Company Abrasive articles and methods of making same
US5573619A (en) * 1991-12-20 1996-11-12 Minnesota Mining And Manufacturing Company Method of making a coated abrasive belt with an endless, seamless backing
US5578096A (en) * 1995-08-10 1996-11-26 Minnesota Mining And Manufacturing Company Method for making a spliceless coated abrasive belt and the product thereof
US5578095A (en) * 1994-11-21 1996-11-26 Minnesota Mining And Manufacturing Company Coated abrasive article
US5584897A (en) * 1994-02-22 1996-12-17 Minnesota Mining And Manufacturing Company Method for making an endless coated abrasive article
US5611825A (en) * 1992-09-15 1997-03-18 Minnesota Mining And Manufacturing Company Abrasive articles and methods of making same
US5673780A (en) * 1996-02-20 1997-10-07 International Automated Systems, Inc. Method of installing a level ball bearing floor
US5677050A (en) * 1995-05-19 1997-10-14 Minnesota Mining And Manufacturing Company Retroreflective sheeting having an abrasion resistant ceramer coating
US5681612A (en) * 1993-06-17 1997-10-28 Minnesota Mining And Manufacturing Company Coated abrasives and methods of preparation
US5744239A (en) * 1996-09-27 1998-04-28 Minnesota Mining And Manufacturing Company Addition of antimicrobial agents to pavement marking materials
US5876268A (en) * 1997-01-03 1999-03-02 Minnesota Mining And Manufacturing Company Method and article for the production of optical quality surfaces on glass
US5888119A (en) * 1997-03-07 1999-03-30 Minnesota Mining And Manufacturing Company Method for providing a clear surface finish on glass
US5910471A (en) * 1997-03-07 1999-06-08 Minnesota Mining And Manufacturing Company Abrasive article for providing a clear surface finish on glass
US5958794A (en) * 1995-09-22 1999-09-28 Minnesota Mining And Manufacturing Company Method of modifying an exposed surface of a semiconductor wafer
US6001522A (en) * 1993-07-15 1999-12-14 Imation Corp. Barrier layer for photoconductor elements comprising an organic polymer and silica
US6040061A (en) * 1992-10-01 2000-03-21 3M Innovative Properties Company Tear resistant multilayer films based on sebacic acid copolyesters and articles incorporating such films
US6121143A (en) * 1997-09-19 2000-09-19 3M Innovative Properties Company Abrasive articles comprising a fluorochemical agent for wafer surface modification
US6132861A (en) * 1998-05-04 2000-10-17 3M Innovatives Properties Company Retroreflective articles including a cured ceramer composite coating having a combination of excellent abrasion, dew and stain resistant characteristics
US6194317B1 (en) 1998-04-30 2001-02-27 3M Innovative Properties Company Method of planarizing the upper surface of a semiconductor wafer
US6231629B1 (en) 1997-03-07 2001-05-15 3M Innovative Properties Company Abrasive article for providing a clear surface finish on glass
US6245833B1 (en) 1998-05-04 2001-06-12 3M Innovative Properties Ceramer composition incorporating fluoro/silane component and having abrasion and stain resistant characteristics
US6265061B1 (en) 1998-05-04 2001-07-24 3M Innovative Properties Company Retroflective articles including a cured ceramer composite coating having abrasion and stain resistant characteristics
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ZA887156B (en) 1990-05-30
CA1329440C (en) 1994-05-10
JPH01138278A (ja) 1989-05-31
DE3882108D1 (de) 1993-08-05
DE3882108T2 (de) 1993-11-18
EP0309276A3 (en) 1990-03-28
JP2756272B2 (ja) 1998-05-25
EP0309276B1 (de) 1993-06-30
EP0309276A2 (de) 1989-03-29

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